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Human Molecular Genetics|April 17, 2018
A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritisMichael J Jurynec, Allen D Sawitzke, Timothy C Beals, et al.Human Heredity|January 5, 2006
Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigreeHilary Coon, Nori Matsunami, Jeff Stevens, et al.Cancers|June 2, 2021
A Rare Variant in <i>ERF</i> (rs144812092) Predisposes to Prostate and Bladder Cancers in an Extended PedigreeLisa Anne Cannon-Albright, Craig Carl Teerlink, Jeff Stevens, et al.The Iowa Orthopaedic Journal|August 16, 2002
Identification and initial characterization of 6,000 expressed sequenced tags (ESTs) from rat normal-growing cartilage and swarm rat chondrosarcoma cDNA librariesJose A Morcuende, Xiao Dong Huang, Jeff Stevens, et al.Gastroenterology|February 6, 2025
Overlap of Genomic and Transcriptomic Genes Identified in Familial Eosinophilic EsophagitisKristina Allen-Brady, Frederic Clayton, Mark W Hazel, et al.Annals of Human Genetics|October 7, 2020
A role for the MEGF6 gene in predisposition to osteoporosisCraig C Teerlink, Michael J Jurynec, Rolando Hernandez, et al.Journal of Neuro-Oncology|May 16, 2024
Detection of tumor-derived cell-free DNA in cerebrospinal fluid using a clinically validated targeted sequencing panel for pediatric brain tumorsRebecca Ronsley, Kristine A Karvonen, Bonnie Cole, et al.International Journal of Cancer|March 14, 2023
A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancerLisa A Cannon-Albright, Craig C Teerlink, Jeff Stevens, et al.Journal of Neurosurgery|November 26, 2022
A likely HOXC4 predisposition variant for Chiari malformationsDouglas L Brockmeyer, Samuel H Cheshier, Jeff Stevens, et al.Birth Defects Research|March 24, 2018
Germline but not somatic de novo mutations are common in human congenital diaphragmatic herniaNori Matsunami, Hari Shanmugam, Lisa Baird, et al.Pageof 4